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Synergistic effect of the responses of different tissues against African swine fever virus

African swine fever is an acute, haemorrhagic fever and contagious disease of pigs caused by African swine fever virus (ASFV), which has a great impact on the pig farming industry and related international trade. Understanding the response processes of various tissues in pigs after ASFV infection ma...

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Autores principales: Fan, Wenhui, Cao, Ying, Jiao, Pengtao, Yu, Ping, Zhang, He, Chen, Teng, Zhou, Xintao, Qi, Yu, Sun, Lei, Liu, Di, Zhu, Hongfei, Liu, Wenjun, Hu, Rongliang, Li, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544764/
https://www.ncbi.nlm.nih.gov/pubmed/34369669
http://dx.doi.org/10.1111/tbed.14283
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author Fan, Wenhui
Cao, Ying
Jiao, Pengtao
Yu, Ping
Zhang, He
Chen, Teng
Zhou, Xintao
Qi, Yu
Sun, Lei
Liu, Di
Zhu, Hongfei
Liu, Wenjun
Hu, Rongliang
Li, Jing
author_facet Fan, Wenhui
Cao, Ying
Jiao, Pengtao
Yu, Ping
Zhang, He
Chen, Teng
Zhou, Xintao
Qi, Yu
Sun, Lei
Liu, Di
Zhu, Hongfei
Liu, Wenjun
Hu, Rongliang
Li, Jing
author_sort Fan, Wenhui
collection PubMed
description African swine fever is an acute, haemorrhagic fever and contagious disease of pigs caused by African swine fever virus (ASFV), which has a great impact on the pig farming industry and related international trade. Understanding the response processes of various tissues in pigs after ASFV infection may help to address current major concerns, such as the exploration of key genes for vaccine development, the cooperative mechanism of the host response and the possibility of establishing active herd immunity. ASFV is able to infect core tissues and is associated with acute death. RNA and protein samples were obtained and verified from five tissues, including the lung, spleen, liver, kidney and lymph nodes. Multiple duplicate samples were quantitatively analyzed by corresponding transcriptomic and proteomic comparison. The results showed that different tissues cooperated in responses to ASFV infection and coordinated the defence against ASFV in the form of an inflammatory cytokine storm and interferon activation. The lung and spleen were mainly involved (dominant) in the innate immune response pathway; the liver and kidney were involved in the metabolic regulatory pathway and the inflammatory response; and the lymph nodes cooperated with the liver to complete energy metabolism regulation. The key pathways and responsive genes in each tissue of the contracted pigs were comprehensively mapped by infectomics, providing further evidence to investigate the complicated tie between ASFV and host cells.
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spelling pubmed-95447642022-10-14 Synergistic effect of the responses of different tissues against African swine fever virus Fan, Wenhui Cao, Ying Jiao, Pengtao Yu, Ping Zhang, He Chen, Teng Zhou, Xintao Qi, Yu Sun, Lei Liu, Di Zhu, Hongfei Liu, Wenjun Hu, Rongliang Li, Jing Transbound Emerg Dis Original Articles African swine fever is an acute, haemorrhagic fever and contagious disease of pigs caused by African swine fever virus (ASFV), which has a great impact on the pig farming industry and related international trade. Understanding the response processes of various tissues in pigs after ASFV infection may help to address current major concerns, such as the exploration of key genes for vaccine development, the cooperative mechanism of the host response and the possibility of establishing active herd immunity. ASFV is able to infect core tissues and is associated with acute death. RNA and protein samples were obtained and verified from five tissues, including the lung, spleen, liver, kidney and lymph nodes. Multiple duplicate samples were quantitatively analyzed by corresponding transcriptomic and proteomic comparison. The results showed that different tissues cooperated in responses to ASFV infection and coordinated the defence against ASFV in the form of an inflammatory cytokine storm and interferon activation. The lung and spleen were mainly involved (dominant) in the innate immune response pathway; the liver and kidney were involved in the metabolic regulatory pathway and the inflammatory response; and the lymph nodes cooperated with the liver to complete energy metabolism regulation. The key pathways and responsive genes in each tissue of the contracted pigs were comprehensively mapped by infectomics, providing further evidence to investigate the complicated tie between ASFV and host cells. John Wiley and Sons Inc. 2021-08-18 2022-07 /pmc/articles/PMC9544764/ /pubmed/34369669 http://dx.doi.org/10.1111/tbed.14283 Text en © 2021 The Authors. Transboundary and Emerging Diseases published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Fan, Wenhui
Cao, Ying
Jiao, Pengtao
Yu, Ping
Zhang, He
Chen, Teng
Zhou, Xintao
Qi, Yu
Sun, Lei
Liu, Di
Zhu, Hongfei
Liu, Wenjun
Hu, Rongliang
Li, Jing
Synergistic effect of the responses of different tissues against African swine fever virus
title Synergistic effect of the responses of different tissues against African swine fever virus
title_full Synergistic effect of the responses of different tissues against African swine fever virus
title_fullStr Synergistic effect of the responses of different tissues against African swine fever virus
title_full_unstemmed Synergistic effect of the responses of different tissues against African swine fever virus
title_short Synergistic effect of the responses of different tissues against African swine fever virus
title_sort synergistic effect of the responses of different tissues against african swine fever virus
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544764/
https://www.ncbi.nlm.nih.gov/pubmed/34369669
http://dx.doi.org/10.1111/tbed.14283
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